Andrew Purchase, Director of Pharmacovigilance & Patient Safety and UK QPPV at ICON sat down with Vivian MacAdden, Senior Manager, Industry Marketing at DistillerSR to discuss the critical role of literature surveillance in the pharmaceutical and biotechnology...
As the Director of Consulting Operations for Maple Health Group, I conduct both targeted and systematic literature reviews (TLRs and SLRs) in addition to working with consultants within my organization to improve the efficiency in which we conduct these reviews. Our...
At our recent webinar, we were joined by Dr. Shirley Sylvester, Therapeutic Area Medical Affairs Leader, Infectious Diseases and Vaccines at Johnson & Johnson, Vardhini Ganesh, Associate Bioinformatician, Immunology - Vaccine at Sanofi, Dr. Richa Goyal Rai,...
In a recent webinar, DistillerSR customers Christa Goode, Director of Clinical and Medical Affairs at Johnson & Johnson, and Sara Garbin, Senior Clinical Development Scientist at Philips, were joined by Dr. Bassil Akra, founder and CEO of AKRA Team GmbH, to...
Dual independent screening in your systematic review process is undoubtedly considered a best practice. But for some research teams, a lack of resources precludes this from being a standard operating procedure. New evidence reinforces the value in dual screening, and...
At our session at MedTech Summit 2021, we were joined by Sara Garbin, Senior Clinical Development Scientist at Philips and Alison Ramsey, Director/Head, Clinical Evaluations at Alcon for an insightful discussion about how leveraging automation can improve manual...
The introduction of new guidelines for the diagnostics industry, outlined by the In-Vitro Diagnostics Regulation (EU) 2017/746 (known as IVDR), imposes significant changes for many manufacturers, who need a robust strategy to adequately support diagnostic products and...
A presentation at the Medical Librarian Association’s 2021 virtual conference brought together Jimmy McColery, Digital Education Specialist at Clarivate, and Jennifer Tetzlaff, DistillerSR’s Epidemiologist-in-Residence, to discuss how their respective solutions help...
Introduction On May 26, 2021, the European Union Medical Device Regulation (EU) 2017/745 (otherwise known as EU-MDR) went into effect for all member states, following a one-year extension due to the COVID-19 pandemic. The implementation of this regulation puts into...
One key component of realizing Evidence-informed decision making (EIDM) is ensuring decision makers have easy access to the best available evidence as quickly as possible. NCCMT does this through several initiatives including offering high-quality resources,...